EVALUATION OF CROSS-REACTING ANTI-HUMAN ANTIBODIES IN THE EUTHYMIC HAIRLESS GUINEA-PIG MODEL (HGP) SUGGESTS THAT THE HGP MAY BE A MODEL FORTHE STUDY OF PROLIFERATIVE SKIN-DISEASE
Kj. Smith et al., EVALUATION OF CROSS-REACTING ANTI-HUMAN ANTIBODIES IN THE EUTHYMIC HAIRLESS GUINEA-PIG MODEL (HGP) SUGGESTS THAT THE HGP MAY BE A MODEL FORTHE STUDY OF PROLIFERATIVE SKIN-DISEASE, Journal of dermatological science, 14(3), 1997, pp. 240-250
Animal models have an important role in cutaneous research. The guinea
pig has proven to be a useful model in a wide spectrum of these cutan
eous studies; however, its usefulness is often compromised by the need
for depilation. A euthymic hairless guinea pig (HGP) model avoids the
problems associated with depilation. Morphologically, as in human ski
n, these animals have a multi-cell-layer epidermis. Proliferation kine
tic studies, as well as documentation of the degree of immunologic cro
ss-reactivity between available antibodies to human cutaneous antigens
, could extend the usefulness of this animal model. We performed a bat
tery of anti-human antibodies on formalin fixed tissue, to a variety o
f antigens present within the skin and on inflammatory cells. These in
cluded CD3, UCHL-1, OPD4, L-26, KP-I, Factor XIIIa, S-100 protein, cyt
okeratin (AE1, AE3 and CK1), CAM 5.2, vimentin, CD 34, Factor VIII, fi
bronectin, SM actin, collagen IV, laminin, Bcl-2, p53, Ki-67, and PCNA
. Cross-reacting antibodies included: CD3 S-100 protein, cytokeratin (
AE1, AE3 and CK1), vimentin, Factor VIII, SM actin, collagen IV, p53,
Ki-67, and PCNA. Although this battery of antibodies is limited, the m
arkedly increased staining of Ki-67 and PCNA within keratinocytes in t
he epidermis as compared to normal human skin reflects a high prolifer
ative rate. In addition, positive staining for p53, Ki-67, and PCNA ma
y be useful in studying effects on cell cycle kinetics and apoptosis.A
lthough inflammatory cells and stromal and basement membrane antibodie
s showed limited cross-reactivity, these as well as the other markers
used in this study, may prove useful in the HGP model. (C) 1997 Elsevi
er Science Ireland Ltd.